methocarbamol

Generic: methocarbamol

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methocarbamol
Generic Name methocarbamol
Labeler a-s medication solutions
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methocarbamol 750 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-1781
Product ID 50090-1781_ee81560c-8542-4384-ae20-9c7ab551c957
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090200
Listing Expiration 2026-12-31
Marketing Start 2013-03-20

Pharmacologic Class

Established (EPC)
muscle relaxant [epc]
Physiologic Effect
centrally-mediated muscle relaxation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500901781
Hyphenated Format 50090-1781

Supplemental Identifiers

RxCUI
197944
UNII
125OD7737X
NUI
N0000175730 N0000175737

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name methocarbamol (source: ndc)
Generic Name methocarbamol (source: ndc)
Application Number ANDA090200 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 750 mg/1
source: ndc
Packaging
  • 20 TABLET in 1 BOTTLE (50090-1781-0)
  • 40 TABLET in 1 BOTTLE (50090-1781-1)
  • 28 TABLET in 1 BOTTLE (50090-1781-2)
  • 30 TABLET in 1 BOTTLE (50090-1781-3)
  • 60 TABLET in 1 BOTTLE (50090-1781-4)
  • 100 TABLET in 1 BOTTLE (50090-1781-6)
  • 12 TABLET in 1 BOTTLE (50090-1781-7)
source: ndc

Packages (7)

Ingredients (1)

methocarbamol (750 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ee81560c-8542-4384-ae20-9c7ab551c957", "openfda": {"nui": ["N0000175730", "N0000175737"], "unii": ["125OD7737X"], "rxcui": ["197944"], "spl_set_id": ["2c1f5949-d771-45c6-8d8a-5e1942c853dc"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (50090-1781-0)", "package_ndc": "50090-1781-0", "marketing_start_date": "20150416"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (50090-1781-1)", "package_ndc": "50090-1781-1", "marketing_start_date": "20150416"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (50090-1781-2)", "package_ndc": "50090-1781-2", "marketing_start_date": "20150416"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-1781-3)", "package_ndc": "50090-1781-3", "marketing_start_date": "20150416"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (50090-1781-4)", "package_ndc": "50090-1781-4", "marketing_start_date": "20150416"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-1781-6)", "package_ndc": "50090-1781-6", "marketing_start_date": "20200302"}, {"sample": false, "description": "12 TABLET in 1 BOTTLE (50090-1781-7)", "package_ndc": "50090-1781-7", "marketing_start_date": "20150416"}], "brand_name": "Methocarbamol", "product_id": "50090-1781_ee81560c-8542-4384-ae20-9c7ab551c957", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "50090-1781", "generic_name": "Methocarbamol", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "750 mg/1"}], "application_number": "ANDA090200", "marketing_category": "ANDA", "marketing_start_date": "20130320", "listing_expiration_date": "20261231"}